N-Acenoacenes: synthesis and solid-state properties

Four N-acenoacenes were synthesized and analyzed for their optoelectronic properties and solid-state packings. Two of the regioisomeric acridinoacridines are TIPS-ethynylated, whereas the other pair are Boc- and triflate substituted derivatives. The two TIPS-ethynyldiazaacenoacenes were processed in...

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Hauptverfasser: Wiesner, Thomas (VerfasserIn) , Pardon, Marcel (VerfasserIn) , Maier, Steffen (VerfasserIn) , Rominger, Frank (VerfasserIn) , Freudenberg, Jan (VerfasserIn) , Bunz, Uwe H. F. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2022
In: Chemistry - a European journal
Year: 2022, Jahrgang: 28, Heft: 69
ISSN:1521-3765
DOI:10.1002/chem.202201916
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.202201916
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202201916
Volltext
Verfasserangaben:Thomas Wiesner, Marcel Pardon, Steffen Maier, Frank Rominger, Jan Freudenberg, Uwe Heiko Bunz

MARC

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520 |a Four N-acenoacenes were synthesized and analyzed for their optoelectronic properties and solid-state packings. Two of the regioisomeric acridinoacridines are TIPS-ethynylated, whereas the other pair are Boc- and triflate substituted derivatives. The two TIPS-ethynyldiazaacenoacenes were processed into organic thin-film transistors with saturation hole mobilities reaching 2.9x10‑2cm2 (Vs) ‑1 . 
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